FORM 6-K
Report of Foreign Private Issuer
Pursuant to Rule 13a-16 or 15d-16
of the Securities Exchange Act of 1934
November, 2003
Commission File Number 1-15182
DR. REDDYS LABORATORIES LIMITED
7-1-27, Ameerpet
Hyderabad, Andhra Pradesh 500 016, India
+91-40-23731946
Indicate by check mark whether registrant files or will file annual reports under cover of Form 20-F or Form 40-F.
Form 20-F [X] Form 40-F [ ]
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Indicate by check mark whether by furnishing the information contained in this Form, the registrant is also thereby furnishing the information to the Commission pursuant to Rule 12g3-2(b) under the Securities Exchange Act of 1934.
Yes [ ] No [X]
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Signatures |
Table of Contents
(1) | Press Release, Dr. Reddys receives final approval for AmVaz (Amlodipine Maleate), First Indian Pharmaceutical Company to receive FDA approval for a NDA under Sec. 505(b)(2) of the Federal Food, Drug and Cosmetics Act, November 3, 2003 |
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Dr. Reddys Laboratories Ltd. 7-1-27 Ameerpet Hyderabad 500 016 India |
Tel: 91 40 2373 1946 Fax: 91 40 2373 1955 |
www.drreddys.com |
Dr. Reddys receives final approval for AmVazTM(Amlodipine Maleate)
First Indian Pharmaceutical Company to receive FDA approval for a NDA
under Sec. 505(b)(2) of the Federal Food, Drug and Cosmetics Act
Hyderabad, India, November 3, 2003: Dr. Reddys Laboratories (NYSE:RDY) announced today that the U.S. Food and Drug Administration (FDA) has approved the Companys NDA for AmVaz (Amlodipine Maleate).
Commenting on the development, GV Prasad, CEO, Dr. Reddys Laboratories, said, the final approval, the first for an Indian Pharmaceutical Company, marks a significant milestone for Dr. Reddys, setting the stage for the launch of our first specialty branded product in the United States. We have not made a final decision on the launch date. But we are making all necessary preparations for the launch and are in the process of finalizing a co-promotion partner for AmVaz (Amlodipine Maleate) in the United States.
The Company has active development programs on a number of differentiated compounds in major therapeutic categories and expects additional NDA filings during the current fiscal year.
The Company is also preparing to launch Amlodipine Maleate in Europe upon expiration of the Supplementary Protection Certificate in March 2004.
Dr. Reddys US product pipeline currently comprises 27 ANDAs, 2 NDAs (including Amlodipine Maleate) and 44 DMFs. Of these ANDAs, 20 were submitted under Paragraph IV. During the current fiscal, the Company expects to file 15-18 ANDAs, 15 DMFs and additional NDAs.
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Signatures
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.
Dr. Reddys Laboratories Limited | ||||
(Registrant) | ||||
Date: November 4, 2003 | By: | /s/ Santosh Kumar Nair | ||
(Signature)* | ||||
Santosh Kumar Nair | ||||
Company Secretary |
* Print the name and title of the signing officer under his signature.
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